ANTIMICROBIAL PEPTIDE AS-HEPC3(48-56) OF ACANTHOPAGRUS SCHLEGELII AND METHOD THEREOF

Abstract

The present disclosure discloses an antimicrobial peptide AS-hepc3.sub.(48-56) of Acanthopagrus schlegelii and method thereof. A molecular formula of the antimicrobial peptide AS-hepc3.sub.(48-56) is C.sub.48H.sub.86N.sub.24O.sub.10S.sub.3, and an amino acid sequence of the antimicrobial peptide AS-hepc3.sub.(48-56) is SEQ ID NO: 01.

Claims

1. An antimicrobial peptide AS-hepc3.sub.(48-56) of Acanthopagrus schlegelii, wherein: a molecular formula of the antimicrobial peptide AS-hepc3.sub.(48-56) is C.sub.48H.sub.86N.sub.24O.sub.10S.sub.3, and an amino acid sequence of the antimicrobial peptide AS-hepc3.sub.(48-56) is SEQ ID NO: 01.

2. The antimicrobial peptide AS-hepc3.sub.(48-56) according to claim 1, wherein a molecular weight of the antimicrobial peptide AS-hepc3.sub.(48-56) is 1255.567 Daltons.

3. The antimicrobial peptide AS-hepc3.sub.(48-56) according to claim 1, wherein the antimicrobial peptide AS-hepc3.sub.(48-56) comprises 5 positively charged amino acid residues and 3 cysteine residues.

4. A method for preparing an antimicrobial drug using the antimicrobial peptide AS-hepc3.sub.(48-56) according to claim 1.

5. An antimicrobial drug, comprising: an antimicrobial peptide AS-hepc3.sub.(48-56) of Acanthopagrus schlegelii, wherein an amino acid sequence of the antimicrobial peptide AS-hepc3.sub.(48-56) is SEQ ID NO: 01.

6. The antimicrobial drug according to claim 5, wherein an active ingredient of the antimicrobial drug is the antimicrobial peptide AS-hepc3.sub.(48-56).

7. The antimicrobial drug according to claim 5, wherein the antimicrobial drug is configured to at least one of inhibit or kill at least one of Pseudomonas aeruginosa, Staphylococcus aureus, or Escherichia coli.

8. A method for preparing an antimicrobial drug using the antimicrobial peptide AS-hepc3.sub.(48-56) according to claim 2.

9. A method for preparing an antimicrobial drug using the antimicrobial peptide AS-hepc3.sub.(48-56) according to claim 3.

10. The antimicrobial drug according to claim 6, wherein the antimicrobial drug is configured to at least one of inhibit or kill at least one of Pseudomonas aeruginosa, Staphylococcus aureus, or Escherichia coli.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0021] FIG. 1 illustrates a comparison of antimicrobial resistance of an antimicrobial peptide AS-hepc3.sub.(48-56) of Acanthopagrus schlegelii and antibiotic meropenem against Pseudomonas aeruginosa PAO1, wherein the abscissa represents time (days), and the ordinate represents a ratio of change of a minimum inhibition concentration (MIC) and an initial antimicrobial concentration.

[0022] FIGS. 2A and 2B illustrate cytotoxicity experimental result diagrams of antimicrobial peptide AS-hepc3.sub.(48-56) obtained by an MTS-PMS method, wherein FIG. 2A represents AML12 cells (alpha mouse liver 12 cells), FIG. 2B represents 293T cells, the abscissa represents an AS-hepc3.sub.(48-56) protein concentration (μM), and the ordinate represents a cell proliferation rate (%).

DETAILED DESCRIPTION OF THE EMBODIMENTS

Embodiment 1

[0023] An amino acid sequence of an antimicrobial peptide AS-hepc3.sub.(48-56) of Acanthopagrus schlegelii of this embodiment is as follows.

TABLE-US-00002 (SEQ ID NO: 01) Arg-Arg-Arg-Arg-Cys-Arg-Phe-Cys-Cys

[0024] In this embodiment, the antimicrobial peptide AS-hepc3.sub.(48-56) was synthesized by GL Biochemical (Shanghai) Co., Ltd. by a solid-phase synthesis method, and a purity of the antimicrobial peptide AS-hepc3.sub.(48-56) was more than 95%. Detection information comprising polypeptide molecular weight, HPLC (high-performance liquid chromatograph), etc. were provided, and related physicochemical parameters are shown in Table 1.

TABLE-US-00003 TABLE 1 Physicochemical parameters of antimicrobial peptide AS-hepc3.sub.(48-56) Physicochemical parameter AS-hepc3.sub.(48-56) Number of amino acid residues 9 Molecular weight 1255.567 Da (Daltons) Molecular formula C.sub.48H.sub.86N.sub.24O.sub.10S.sub.3 Isoelectric point 11.40 Net charge +5 Hydrophobicity 44% Total average hydrophilicity −1.356 Protein binding potential energy 2.2 kcal/mol Molar extinction coefficient 187.5

[0025] Referring to Table 1, the antimicrobial peptide AS-hepc3.sub.(48-56) of this embodiment has a small molecular weight, good stability, and high water solubility, and the antimicrobial peptide AS-hepc3.sub.(48-56) is a positively charged cationic polypeptide.

Embodiment 2: Verification of Minimum Inhibition Concentration (MIC) and Minimum Bactericidal Concentration (MBC)

[0026] 1. Strains were as follows: Pseudomonas aeruginosa PAO1, drug-resistant clinical Pseudomonas aeruginosa isolates QZ19121, QZ19122, QZ19123, QZ19124, and QZ19125, drug-resistant clinical Acinetobacter baumannii isolates QZ18050 and QZ18055, clinical isolation of resistant Staphylococcus aureus QZ18090 and QZ18091, drug-resistant clinical Klebsiella pneumoniae isolate QZ18106, and drug-resistant clinical Escherichia coli isolates QZ18109 and QZ18110. Pseudomonas aeruginosa PAO1 was purchased from the China General Microbiological Culture Collection Center, Institute of Microbiology, Chinese Academy of Sciences, and the clinical isolates were from the Laboratory of Second Affiliated Hospital of Fujian Medical University.

[0027] 2. A detailed method is as follows.

[0028] (1) Preserved strains were streaked on MH plates (Mueller-Hinton agar plates) and were cultured at 37° C. overnight;

[0029] (2) A single clone was screened and was cultured in a MH liquid medium (Mueller-Hinton agar liquid medium) at 37° C. and 200 rpm (revolutions per minute) to a logarithmic stage;

[0030] (3) The strains were collected at 5000 g (i.e., a 5000 g centrifugal force) for 2 minutes, the strains were resuspended with a 10 mM (mmol/L) sodium phosphate buffer (pH=7.4), and the strains were finally diluted with the MH liquid medium to enable a final concentration of the strains to be 5×10.sup.5 cfu/mL;

[0031] (4) Synthesized powder of the antimicrobial peptide AS-hepc3.sub.(48-56) was dissolved in sterile Milli-Q water, and a peptide concentration (i.e., a concentration of the antimicrobial peptide AS-hepc3.sub.(48-56)) was diluted to 2 μM, 4 μM, 8 μM, 16 μM, 32 μM, or 64 μM in double ratios; and

[0032] (5) On a polypropylene sterile 96-well culture plate, each test strain was arranged into a blank control group, a negative control group, and a test group, and three parallel groups of each test group were as follows: [0033] a) Blank control group: 50 μL of test peptide sample (i.e., the antimicrobial peptide AS-hepc3.sub.(48-56)) and 50 μL of medium (i.e., the Mueller-Hinton agar liquid medium); [0034] b) Negative control group: 50 μL of sterile Milli-Q water and 50 μL of strain suspension; and [0035] c) Test group: 50 μL of test peptide sample and 50 μL of the strain suspension.

[0036] The polypropylene sterile 96-well culture plate was placed in a 37° C. incubator for 18-24 hours, and MIC results in the test group were observed. After the test group was pipetted and mixed, an appropriate amount of the strain was drawn and spread on the MH plate and was cultured at 37° C. overnight, and MBC results were observed.

[0037] 3. The MIC and MBC results of the antimicrobial peptide AS-hepc3.sub.(48-56) are shown in Table 2.

TABLE-US-00004 TABLE 2 Antimicrobial activity of the antimicrobial peptide AS-hepc3.sub.(48-56) Strain Microorganism NO. MIC MBC Pseudomonas aeruginosa P. aeruginosa CGMCC: 4-8 8 PAO1 1.12483 Pseudomonas aeruginosa P. aeruginosa QZ19121 4-8 16 Pseudomonas aeruginosa P. aeruginosa QZ19122 4-8 16 Pseudomonas aeruginosa P. aeruginosa QZ19123 4-8 16 Pseudomonas aeruginosa P. aeruginosa QZ19124 4-8 16 Pseudomonas aeruginosa P. aeruginosa QZ19125  8-16 16 Acinetobacter baumannii A. baumannii QZ18050 >32 >32 Acinetobacter baumannii A. baumannii QZ18055 >32 >32 Staphylococcus aureus S. aureus QZ18090 4-8 8 Staphylococcus aureus S. aureus QZ18091 4-8 8 Klebsiella pneumoniae K. pneumoniae QZ18106 >32 >32 Escherichia coli E. coli QZ18109 4-8 16 Escherichia coli E. coli QZ18110 4-8 8

[0038] Annotations: MIC: minimum inhibitory concentration (μM), which is represented by a-b; a is a maximum peptide concentration at which a growth of the strain can be observed by naked eyes, and b is a minimum peptide concentration at which no growth of the strain can be observed by the naked eyes. MBC: Minimum bactericidal concentration (μM), which is a concentration that kills 99.9% of microbes.

Embodiment 3: Comparative Experiments of Drug Resistance

[0039] 1. Comparison of the antimicrobial peptide AS-hepc3.sub.(48-56) and antibiotic meropenem against Pseudomonas aeruginosa PAO1. Pseudomonas Aeruginosa PAO1 was purchased from the China General Microbiological Culture Collection Center, Institute of Microbiology, Chinese Academy of Sciences.

[0040] A detailed method is as follows:

[0041] (1) Preserved Pseudomonas aeruginosa PAO1 was streaked on MH plates and was cultured at 37° C. overnight;

[0042] (2) A single clone was screened and was cultured in MH liquid medium at 37° C. and 200 rpm to a logarithmic stage;

[0043] (3) The strain was corrected at 5000 g for 2 minutes, the strain was resuspended in 10 mM sodium phosphate buffer (pH=7.4), and the strain was finally diluted with a mixture of the 10 mM sodium phosphate buffer and the MH liquid medium to enable a final concentration of the stain to be 5×10.sup.5 cfu/mL;

[0044] (4) Synthesized powder of the antimicrobial peptide AS-hepc3.sub.(48-56) was dissolved in sterile Milli-Q water, and a peptide concentration was diluted to 8 μM, 12 μM, 16 μM, 24 μM, 32 μM, 48 μM, 64 μM, or 96 μM in double ratios;

[0045] (5) Antibiotic meropenem powder was dissolved in sterile Milli-Q water to configure a 5 mg/mL reserved solution, filtered by a 0.22 μm filter membrane, and diluted to different work concentrations being 0.0625 μg/mL, 0.125 μg/mL, 0.25 μg/mL, 0.5 μg/mL, 1 μg/mL, 2 μg/mL, 4 μg/mL, 8 μg/mL, 16 μg/mL, 32 μg/mL, 48 μg/mL, 64 μg/mL, 96 μg/mL, 128 μg/mL, 192 μg/mL, 256 μg/mL, or 512 μg/mL; and

[0046] (6) On a 96-well cell culture plate, each test strain was arranged into a blank control group, a negative control group, and a test group, and three parallel groups of each test group were as follows: [0047] a) Blank control group: 50 μL of test peptide sample and 50 μL of medium; [0048] b) Negative control group: 50 μL of sterile Milli-Q water and 50 μL of strain suspension; and [0049] c) Test group: 50 μL of the test peptide sample and 50 μL of the strain suspension.

[0050] The 96-well cell culture plate was placed in a 37° C. incubator and was cultured for 18-24 hours, and MIC results in the test group were observed. The strain having the maximum peptide concentration at which the growth of the strain could be observed was repeatedly diluted thousand-fold, and 50 μL was repeatedly taken for a next generation of antimicrobial experiments for 150 generations.

[0051] 3. The results are shown in FIG. 1. When the antibiotic meropenem was used to act on Pseudomonas aeruginosa PAO1, an anti-Pseudomonas aeruginosa MIC value of the antibiotic meropenem was increased to 4 times an initial MIC value after 3 days. The anti-Pseudomonas aeruginosa MIC value was increased to 16 times the initial MIC value and was increased continually after 10 days of continuous use. The anti-Pseudomonas aeruginosa MIC value increased 1024 times after 90 days of use, which indicates that Pseudomonas aeruginosa has high drug resistance to the antibiotic meropenem. However, when the antimicrobial peptide AS-hepc3.sub.(48-56) was used to act on Pseudomonas aeruginosa PAO1, the anti-Pseudomonas aeruginosa MIC value of the antimicrobial peptide AS-hepc3.sub.(48-56) was only twice of the initial MIC value after 150 days of continuous use. There was no significant change, which indicates that Pseudomonas aeruginosa has no obvious drug-resistant effect on the antimicrobial peptide AS-hepc3.sub.(48-56).

Embodiment 4: Detection of Cytotoxicity

[0052] 1. Mouse hepatocytes (AML12) (mouse liver cells) and human kidney epithelial cells (293T) were selected to detect a cytotoxicity of the antimicrobial peptide AS-hepc3.sub.(48-56).

[0053] 2. A detailed method is as follows.

[0054] (6) Well-grown mouse hepatocytes (AML12) and human kidney epithelial cells (293T) were collected, a cell concentration was adjusted to 10.sup.3-10.sup.4 cells/mL, the cells were evenly blown, and 100 μL of strain suspension was placed in each well of a 96-well cell culture plate and was static cultured at a condition of 37° C. and 0.5% CO.sub.2. More than 50% of the strains were adhered to a wall.

[0055] (7) The medium is carefully sucked out, a corresponding medium comprising different concentrations (0 μM, 40 μM, or 80 μM) was added and was static cultured for 24 hours at a condition of 37° C. and 0.5% CO.sub.2.

[0056] (8) After 20 μL of MTS-PMS solution was added and was incubated for 3 hours in the dark, an OD.sub.492 value (optical density reading at 492 nm wavelength) was detected by a microplate reader to evaluate the cytotoxicity of the antimicrobial peptide AS-hepc3.sub.(48-56).

[0057] 3. The results are shown in FIG. 2.

[0058] In a condition of 5 times and 10 times MIC (40 μM and 80 μM), after the antimicrobial peptide AS-hepc3.sub.(48-56) and AML12 cells (FIG. 2A) and 293T cells (FIG. 2B) were co-incubated for 24 hours, a cell survival rate of the test group was more than 95% compared with the control group, which indicated that the antimicrobial peptide AS-hepc3.sub.(48-56) has no cytotoxicity.

[0059] The aforementioned embodiments are merely some embodiments of the present disclosure, and the scope of the disclosure is not limited thereto. Thus, it is intended that the present disclosure cover any modifications and variations of the presently presented embodiments provided they are made without departing from the appended claims and the specification of the present disclosure.